510(k) K210037 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Pluski Safe 1 Safety IV Catheter
| Applicant | Mediplus (India) Limited, Bahadurgarh, IN |
| Decision | Substantially Equivalent, Mar 25, 2022 |
| Received | Jan 6, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210037
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.